Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.08 (G)
Location

Chromosome 1:161230796 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs59634807, rs17397854

HGVS names

This variant has 33 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 45 transcripts, has 3761 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays